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	<title>Recombinant Enzyme &#8211; Tinzyme</title>
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		<title>Recombinant PNGase F</title>
		<link>https://www.tinzyme.com/recombinant-enzyme/recombinant-pngase-f/</link>
		
		<dc:creator><![CDATA[tinzyme]]></dc:creator>
		<pubDate>Tue, 24 Mar 2026 07:05:26 +0000</pubDate>
				<category><![CDATA[Recombinant Enzyme]]></category>
		<category><![CDATA[PSE109]]></category>
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					<description><![CDATA[PSE109, Recombinant PNGase F. N-glycosidase F (PNG...]]></description>
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<p><a href="https://www.tinzyme.com/man/PSE109.pdf" target="_blank" rel="noreferrer noopener">Manual</a></p>



<p><strong>Product Number: PSE109</strong></p>



<p><strong>Shipping and Storage</strong></p>



<ol class="wp-block-list">
<li>Storage temperature: -20±5℃ for storage</li>



<li>Validity period: 2 years.</li>
</ol>



<p><strong>Component</strong></p>



<figure class="wp-block-table"><table class="has-fixed-layout"><tbody><tr><td>Component<strong></strong></td><td>PSE109</td></tr><tr><td>PNGase F</td><td>30μL</td></tr><tr><td>10×Buffer 1</td><td>1mL</td></tr><tr><td>10×Buffer 2</td><td>1mL</td></tr><tr><td>NP-40</td><td>1mL</td></tr></tbody></table></figure>



<p><strong>Description</strong></p>



<p>N-glycosidase F (PNGase F) is an effective amidase produced by recombinant Escherichia coli with cloned genes encoding the enzyme. It can cleave the N-sugar chain on glycoproteins, helping to generate carbohydrate free peptides and oligosaccharides with di-N-acetyl chitosan units. N-glycosidase F is the most effective method for removing almost all N-sugar chains from glycoproteins. The product can remove all complex, heterozygous, and high mannose sugar chains from antibodies and their fusion proteins, but if there are alpha 1,3-linked fucose residues in the core structure (often expressed in plant and insect cells as immunoglobulins), they cannot be cleaved. Obtaining accurate N-sugar chain distribution in the shortest possible time is crucial for effective process control. N-glycosidase F is an optimized reagent that can rapidly deglycosylate antibodies and fusion proteins within a few minutes. All N-sugar chains can be released quickly and without preference, and can be directly subjected to downstream chromatography or mass spectrometry analysis to quickly determine the glycosylation of antibodies.</p>



<p><strong>Active definition</strong></p>



<p>Unit enzyme activity is defined as the amount of enzyme required to remove over 95% of sugar chains from 10μg denatured RNase B within 1 hour in a 10μL reaction system at 37℃.</p>



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<h4 class="wp-block-heading"><strong>Get a quote now</strong></h4>



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